United States · FDA National Drug Code directory
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A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 10742-3051_43fde22f-2a7f-7b72-e063-6294a90a3254
- Product NDC
- 10742-3051
- Form
- OINTMENT
- Composition / generic term
- dimethicone, octinoxate, octisalate, oxybenzone
- Labeler
- The Mentholatum Company
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start / end (source format)
- 19971119
- Source listing expiry
- 20261231
Source-listed ingredients
- DIMETHICONE — 20 mg/g
- OCTINOXATE — 75 mg/g
- OCTISALATE — 30 mg/g
- OXYBENZONE — 30 mg/g
These values do not establish equivalence or a dose recommendation.
Packages
- 1 TUBE in 1 BLISTER PACK (10742-3051-1) / 2 g in 1 TUBE · 10742-3051-1
- 2 g in 1 TUBE (10742-3051-2) · 10742-3051-2
- 3 TUBE in 1 BLISTER PACK (10742-3051-3) / 2 g in 1 TUBE · 10742-3051-3
- 2 TUBE in 1 BLISTER PACK (10742-3051-9) / 2 g in 1 TUBE · 10742-3051-9
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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